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Practice inspection
The Infection Protection Act requires optional infection-hygiene monitoring. The Medical Devices Act also requires the monitoring of all areas in which medical devices are marketed, operated or used or in which sterile or low-germ medical devices are processed. This monitoring is carried out by the responsible authorities according to the structures at the state level. One of the monitoring instruments is the practice inspection, which can be event-related, but in the majority of cases is not event-related.
